Deeds J, Cronin F, Duncan L M
Millennium Predictive Medicine, Cambridge, MA, USA.
Hum Pathol. 2000 Nov;31(11):1346-56.
The melanocyte-specific gene Melastatin (MLSN1) shows an inverse correlation of mRNA expression with metastatic potential in human and murine cell lines in vitro. Melastatin mRNA expression in primary cutaneous melanoma also has been found to correlate with disease-free survival. The histologic patterns of Melastatin mRNA expression in nevi, primary melanoma, and melanoma metastases have not been described previously. Using in situ hybridization with (35)S-labeled probes, we examined Melastatin mRNA expression in 64 cases of normal skin, benign melanocytic nevi, primary cutaneous melanomas, and melanoma metastases. Ubiquitous melanocytic expression of Melastatin mRNA was observed in all benign melanocytic proliferations (14 of 14), although some nevi showed a gradient of reduced Melastatin expression with increased dermal depth (3 of 14). Uniform expression of Melastatin mRNA was observed in 49% of primary cutaneous melanomas (18 of 37 cases, including 1 case of in situ melanoma). Melastatin mRNA loss by a portion of the melanoma was identified in 53% of the invasive melanoma samples (19 of 36) and 100% of the melanoma metastases (11 of 11). Primary melanomas without mRNA loss ranged in thickness from 0.17 to 2.75 mm (median, 0.5 mm; mean, 0.73 mm), whereas tumors that showed Melastatin mRNA down-regulation ranged in thickness from 0.28 to 5.75 mm (median, 1.7 mm; mean, 2.13 mm). A focal aggregate or nodule of melanoma cells without detectable signal was the most commonly observed pattern of Melastatin loss (13 of 19 cases), whereas complete loss of Melastatin mRNA expression by all of the dermal melanoma cells was observed in only 4 of the 19 cases. Two invasive melanomas displayed a scattered, nonfocal pattern of Melastatin mRNA loss. Of the 11 melanoma metastases examined, 64% displayed focal Melastatin mRNA loss, and 36% had complete loss of Melastatin mRNA expression. We observed several patterns of Melastatin mRNA expression in primary melanoma that may be distinguished from expression in benign melanocytic nevi. Melastatin mRNA expression appears to correlate with melanocytic tumor progression, melanoma tumor thickness, and the potential for melanoma metastasis. HUM PATHOL 31:1346:1356.
黑素细胞特异性基因黑素瘤抑制因子(MLSN1)在体外人源和鼠源细胞系中显示出mRNA表达与转移潜能呈负相关。原发性皮肤黑素瘤中黑素瘤抑制因子mRNA表达也已被发现与无病生存期相关。痣、原发性黑素瘤和黑素瘤转移灶中黑素瘤抑制因子mRNA表达的组织学模式此前尚未见描述。我们使用含(35)S标记探针的原位杂交技术,检测了64例正常皮肤、良性黑素细胞痣、原发性皮肤黑素瘤及黑素瘤转移灶中黑素瘤抑制因子mRNA的表达情况。在所有良性黑素细胞增殖病变(14例中的14例)中均观察到黑素瘤抑制因子mRNA在黑素细胞中普遍表达,不过部分痣(14例中的3例)显示随着真皮深度增加黑素瘤抑制因子表达呈递减梯度。49%的原发性皮肤黑素瘤(37例中的18例,包括1例原位黑素瘤)中观察到黑素瘤抑制因子mRNA表达一致。在53%的浸润性黑素瘤样本(36例中的19例)和100%的黑素瘤转移灶(11例中的11例)中发现部分黑素瘤存在黑素瘤抑制因子mRNA缺失。无mRNA缺失的原发性黑素瘤厚度范围为0.17至2.75mm(中位数为0.5mm;平均值为0.73mm),而显示黑素瘤抑制因子mRNA下调的肿瘤厚度范围为0.28至5.75mm(中位数为1.7mm;平均值为2.13mm)。黑素瘤细胞的局灶性聚集或结节且无可检测信号是最常观察到的黑素瘤抑制因子缺失模式(19例中的13例),而在19例中仅有4例观察到所有真皮黑素瘤细胞均完全缺失黑素瘤抑制因子mRNA表达。2例浸润性黑素瘤表现出黑素瘤抑制因子mRNA缺失的散在、非局灶性模式。在所检测的11例黑素瘤转移灶中,64%表现为局灶性黑素瘤抑制因子mRNA缺失,36%完全缺失黑素瘤抑制因子mRNA表达。我们在原发性黑素瘤中观察到几种黑素瘤抑制因子mRNA表达模式,这些模式可能与良性黑素细胞痣中的表达模式有所不同。黑素瘤抑制因子mRNA表达似乎与黑素细胞肿瘤进展、黑素瘤肿瘤厚度以及黑素瘤转移潜能相关。《人类病理学》31:1346:1356。